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促红细胞生成素对晚期卵巢癌经紫杉醇化疗所致神经毒性损伤的保护作用研究 被引量:4

Protection Role of EPO in Neurovirulent Damages Caused by Paclitaxel Chemotherapy in Patients with Advanced Ovarian Cancers
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摘要 目的探讨促红细胞生成素(EPO)对晚期(Ⅲ~Ⅳ期)卵巢癌经紫杉醇化疗后诱发的神经毒性损伤的保护作用。方法选取2009年2月—2012年3月襄阳市中心医院收治的Ⅲ~Ⅳ期卵巢癌患者124例,根据其是否接受EPO治疗及接受治疗的时间分为早期EPO组、晚期EPO组、非EPO组。根据癌症治疗功能评估/妇科肿瘤神经毒性问卷(FACT/GOG-NTX问卷)评分对3组患者行神经毒性评估。比较3组患者神经毒性分级、最早出现神经毒性损伤的时间以及累积紫杉醇用量;比较早期EPO组不同贫血分级患者的神经毒性损伤分级。结果 3组患者神经毒性分级间差异有统计学意义(H=6.862,P=0.032)。早期EPO组不同贫血分级患者的神经毒性损伤分级间差异有统计学意义(u=-3.810,P〈0.05)。早期EPO组发生神经毒性损伤最早时间〔(12.3±2.2)周〕长于晚期EPO组〔(10.7±1.6)周〕及非EPO组〔(7.7±1.2)周,P〈0.05〕。早期EPO组最早发生神经毒性损伤时紫杉醇用量平均为(785.3±67.5)mg,高于晚期EPO组〔(511.6±61.7)mg〕及非EPO组〔(354.2±47.5)mg,P〈0.05〕。结论EPO能够有效减轻以紫杉醇为基础化疗的Ⅲ~Ⅳ期卵巢癌患者神经毒性,早期应用EPO效果更显著。 Objective To explore the role of erythropoietin( EPO) in neurovirulent damages( NVD) caused by paclitaxel chemotherapy in patients with advanced ovarian cancers( AOC). Methods A total of 124 Ⅲ- Ⅳ stage AOC patients admitted to Center Hospital of Xiangyang from February 2009 to March 2012 were divided,according to receiving EPO treatment or not,into groups early EPO,advanced EPO,non- EPO. FACT /GO- NTX questionnaire was used to evaluate the neurovirulence of 3 groups. The neurovirulence,time of NVD appearance,accumulated paclitaxel were compared among 3 groups. NVDs compared between patients with different grades of anemia in EPO group. Results The incidences of NVD of groups early EPO,advanced EPO,non- EPO were 24. 4%( 10 /41),42. 5%( 17 /40),53. 5%( 23 /43),respectively,the difference was significant( H = 6. 862,P = 0. 032). There was difference in incidences of different grades of NVD among 3 groups( P 0. 05). There was difference in NVD incidence between patients with different grades of anemia in early EPO group( u =- 3. 810,P 0. 05). The earliest time of neurovirulence occurrence was longer in early EPO group 〔( 12. 3 ± 2. 2) weeks〕than in groups advanced EPO 〔( 10. 7 ± 1. 6) weeks〕,non- EPO 〔( 7. 7 ± 1. 2) weeks,P 0. 05〕. The mean paclitaxel dosage was( 785. 3 ± 67. 5) mg in early EPO group at earliest time of neurovirulence occurrence,higher than in groups advanced EPO 〔( 511. 6 ± 61. 7) mg〕,non- EPO 〔( 354. 2 ± 47. 5) mg,P 0. 05〕. Conclusion EPO can reduce the NVD caused by paclitaxel chemotherapy in Ⅲ- Ⅳ AOC patients. Early use of EPO is of more remarkable effects.
出处 《中国全科医学》 CAS CSCD 北大核心 2014年第29期3453-3456,共4页 Chinese General Practice
基金 湖北省自然科学基金资助项目(2012FFB01904)
关键词 红细胞生成素 卵巢肿瘤 神经毒性 紫杉醇 Erythropoietin Ovarian neoplasms Neurotoxicity Paclitaxel
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参考文献16

  • 1Pecorelli S, Favalli G, Gadducci A, et al. Phase m trim of observa- tion versus six courses of paclitaxel in patients with advanced epithelial o- varian cancer in complete response after six courses of paclitaxel/plati- num- based chemotherapy: final results of the after-6 protocol 1 [J]. J Clin Oncol, 2009, 27 (28) : 4642 -4648.
  • 2Hurt JD, Richardson DL, Seamon LG, et al. Sustained progression - free survival with weekly paclitaxel and bevacizumab in recurrent ovarian cancer [J]. Gynecol Oncol, 2009, 115 (3): 396-400.
  • 3Green H, Soderkvist P, Rosenberg P, et al. Pharmacogenetic studies of paclitaxel in the treatment of ovarian cancer [ J]. Basic Clin Pharma- col Toxicol, 2009, 104 (2): 130-137.
  • 4Pectasides D, Xiros N, Papaxoinis G, et al. Gemcitabine and pegylat- ed liposomal doxorubicin alternating with cisplatin plus cyclophosphamide in platinum refractory/resistant, paclitaxel - pretreated, ovarian carci- noma [J]. Gynecol Oncol, 2008, 108 (1): 47-52.
  • 5Bianchi R, Buyukakilli B, Brines M, et al. Erythropoietin both pro- teets from and reverses experimental diabetic neuropathy [ J]. Proc Natl Acad Sci USA, 2004, 101 (3) : 823 -828.
  • 6Le T, Hopkins L, Baines KA, et al. Prospective evaluations of contin- uous weekly paclitaxel regimen in recurrent platinum - resistant epithelial ovarian cancer [J]. Gynecol Oncol, 2006, 102 (1) : 49 -53.
  • 7Bell J, Brady MF, Young RC, et al. Randomized phase iii trial of three versus six cycles of adjuvant.carboplatin and paclitaxel in early stage epithelial ovarian carcinoma: a gynecologic oncology group study [J]. Gynecol Oncol, 2006, 102 (3) : 432 -439.
  • 8Vasey PA, Jayson GC, Gordon A, et al. Phase iii randomized trial of docetaxel- carboplatin versus paclitaxel -carboplatin as first- line chemotherapy for ovarian carcinoma [ J ]. J Natl Cancer Inst, 2004, 96 (22): 1682 -1691.
  • 9Doi D, Ota Y, Konishi H, et al. Evaluation of the neurotoxicity of pa- clitaxel and carboplatin by current perception threshold in ovarian cancer patients [J]. J Nippon Med Sch, 2003, 70 (2) : 129 -134.
  • 10Xiao WH, Bennett GJ. Chemotherapy - evoked neuropathic pain : ab- normal spontaneous dischargd in a - fiber and c - fiber primary afferent neurons and its suppression by acetyl - L - carnitine [ J :. Pain, 2008, 135 (3): 262-270.

同被引文献22

  • 1焦旭文,王国平,李军平,韩怀钦,马新伟,侯宝林,张海博.EPO对大鼠腰神经根慢性压迫性损伤的保护作用[J].宁夏医科大学学报,2013,35(11):1199-1203. 被引量:3
  • 2舒进忠,谭诗生.紫杉醇联合顺铂腹腔灌注治疗晚期卵巢癌的临床疗效及其对免疫调节作用的研究[J].中国生化药物杂志,2014,34(2):130-132. 被引量:34
  • 3张录民,赵维,刘国津.乳腺癌患者血清中CEA和CA153的表达及临床意义[J].第四军医大学学报,2007,28(4):307-309. 被引量:17
  • 4Li J,Dowdy S,Tipton T,et al.HE4 as a biomarker for ovarian and endometrial cancer management[J].Expert Rev Mol Diagn,2009,9(6):555-566.
  • 5Erkan kaptanoglu,Ihsan Solaroglu,Ozerk Okutan,et al.Erythropoietin exerts neuroprotection after acute spinal cord injury in rats:effect on lipid peroxidation and early ultra-structural findings[J].Neurosurgical Review,2004,27(2):113-120.
  • 6Wani MC,Taylor HL,Wall ME,et al.Plant antitumor a-gents VI isolation and structure of taxol,a novel antileukemic and antitumor agent from Taxus brevifolia[J].J Am Chem Soc,1971,93(9):2325-2327.
  • 7Shimozuma K,Ohashi Y,Takeuchi A,et al.Taxane-induced peripheral neuropathy and health-related quality of life in postoperative breast cancer patients undergoing adjuvant chemotherapy:N-SAS BC 02,a randomized clinical trial[J].Support Care Cancer,2012,20(12):3355-3364.
  • 8Beijers AJ,Jongen JL,Vreugdenhil G.Chemotherapy-induced neurotoxicity:the value of neuroprotective strategies[J].Neth J Med,2012,70(1):18-25.
  • 9Kothari R,Nagel C,Koopmeiners JS,et al.The effect of age on the tolerability of intraperitoneal chemotherapy,complication rate,and surviral in patients with ovarian cancer[J].Gynecol Oncol,2010,119(3);491-495.
  • 10冯亚高,洪光祥.促红细胞生成素及其受体神经营养和神经保护作用研究进展[J].华北国防医药,2009,21(5):72-74. 被引量:1

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